Harvard Catalyst Profiles

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Emanuela Marchese, Ph.D.

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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Caterino M, Gelzo M, Sol S, Fedele R, Annunziata A, Calabrese C, Fiorentino G, D'Abbraccio M, Dell'Isola C, Fusco FM, Parrella R, Fabbrocini G, Gentile I, Andolfo I, Capasso M, Costanzo M, Daniele A, Marchese E, Polito R, Russo R, Missero C, Ruoppolo M, Castaldo G. Dysregulation of lipid metabolism and pathological inflammation in patients with COVID-19. Sci Rep. 2021 02 03; 11(1):2941. PMID: 33536486.
    Citations: 10     Fields:    Translation:Humans
  2. Cervesato A, Raucci R, Buononato D, Marchese E, Capolongo G, Perna A, Capasso G, Zacchia M. [Application of proteomics and metabolomics to study inherited kidney disorders: from big data to precision medicine]. G Ital Nefrol. 2020 Dec 07; 37(6). PMID: 33295706.
    Citations: 1     Fields:    Translation:HumansAnimals
  3. Zacchia M, Blanco FDV, Torella A, Raucci R, Blasio G, Onore ME, Marchese E, Trepiccione F, Vitagliano C, Iorio VD, Alessandra P, Simonelli F, Nigro V, Capasso G, Viggiano D. Urine concentrating defect as presenting sign of progressive renal failure in Bardet-Biedl syndrome patients. Clin Kidney J. 2021 Jun; 14(6):1545-1551. PMID: 34084454.
    Citations:    
  4. Zacchia M, Marchese E, Trani EM, Caterino M, Capolongo G, Perna A, Ruoppolo M, Capasso G. Proteomics and metabolomics studies exploring the pathophysiology of renal dysfunction in autosomal dominant polycystic kidney disease and other ciliopathies. Nephrol Dial Transplant. 2020 11 01; 35(11):1853-1861. PMID: 31219585.
    Citations: 4     Fields:    Translation:HumansAnimalsCells
  5. Marchese E, Ruoppolo M, Perna A, Capasso G, Zacchia M. Exploring Key Challenges of Understanding the Pathogenesis of Kidney Disease in Bardet-Biedl Syndrome. Kidney Int Rep. 2020 Sep; 5(9):1403-1415. PMID: 32954066.
    Citations: 4     
  6. De Pasquale V, Costanzo M, Siciliano RA, Mazzeo MF, Pistorio V, Bianchi L, Marchese E, Ruoppolo M, Pavone LM, Caterino M. Proteomic Analysis of Mucopolysaccharidosis IIIB Mouse Brain. Biomolecules. 2020 02 26; 10(3). PMID: 32111039.
    Citations: 7     Fields:    Translation:Animals
  7. Caterino M, Ruoppolo M, Villani GRD, Marchese E, Costanzo M, Sotgiu G, Dore S, Franconi F, Campesi I. Influence of Sex on Urinary Organic Acids: A Cross-Sectional Study in Children. Int J Mol Sci. 2020 Jan 16; 21(2). PMID: 31963255.
    Citations: 10     Fields:    Translation:Humans
  8. Villani GRD, Albano L, Caterino M, Crisci D, Di Tommaso S, Fecarotta S, Fisco MG, Frisso G, Gallo G, Mazzaccara C, Marchese E, Nolano A, Parenti G, Pecce R, Redi A, Salvatore F, Strisciuglio P, Turturo MG, Vallone F, Ruoppolo M. Hypermethioninemia in Campania: Results from 10?years of newborn screening. Mol Genet Metab Rep. 2019 Dec; 21:100520. PMID: 31641591.
    Citations:    
  9. Costanzo M, Cevenini A, Marchese E, Imperlini E, Raia M, Del Vecchio L, Caterino M, Ruoppolo M. Label-Free Quantitative Proteomics in a Methylmalonyl-CoA Mutase-Silenced Neuroblastoma Cell Line. Int J Mol Sci. 2018 Nov 13; 19(11). PMID: 30428564.
    Citations: 10     Fields:    Translation:HumansCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.